DEL17P13.1

Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.[2][3]

DEL17P13.1
Identifiers
Aliases	C17DELp13.1Chromosome 17p13.1 deletion syndrome
External IDs	GeneCards:
Orthologs
Species	Human	Mouse
Entrez	100653374	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	[1]	n/a
Wikidata
View/Edit Human

References

1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
2. "Entrez Gene: Chromosome 17p13.1 deletion syndrome".
3. Carvalho CM, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, et al. (November 2014). "Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes". American Journal of Human Genetics. 95 (5): 565–78. doi:10.1016/j.ajhg.2014.10.006. PMC 4225592. PMID 25439725.